Very long-term remission in behcet's disease following withdrawal of anti-TNF treatment exceeds relapses: a reappraisal of an outcome study.

IF 3.2 3区 医学 Q2 RHEUMATOLOGY
Aikaterini Arida, Nikos Markomichelakis, George E Fragoulis, Petros P Sfikakis
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引用次数: 0

Abstract

Background: Introduction of anti-TNF treatment has greatly improved prognosis of Behcet's disease (BD). Withdrawal of anti-TNF treatment in chronic inflammatory arthritis or bowel disease has been associated with sustained remission in subsets of patients. Herein, we examined the probability of very long-term quiescence after withdrawal of TNF inhibitors in BD.

Methods: Retrospective longitudinal outcome single-center study focusing on BD patients who discontinued successful ant-TNF treatment since 2001. Endpoint was their proportion with sustained clinical remission for 5 years after withdrawal.

Results: Thirty-three patients with severe BD refractory to non-biologic treatment (mean age 47.5 ± 11.5 years, 55% men) achieved TNF inhibitor-induced remission for a median of 2 years (IQR [1-2.6]). TNF inhibitors had been given for sight-threatening disease (28/33, 82%), for mucocutaneous (3/33), central nervous system (2/33) and gastrointestinal involvement (1/33). After withdrawal, BD remained in remission in 15/33 patients for 6.6 to 20.6 years (mean 13.5 ± 3.8). Conversely, 18/33 patients relapsed after a median of 9.5 months [IQR 8-12, range 4-32] following withdrawal but retreatment with TNF inhibitors was effective in 13/18. Of them, 9/13 discontinued for a second time and achieved again the study's endpoint, remaining in remission for median of 7.4 years ([IQR 5-9.3, range 5-15 years). Study's end-point was met by 24/33 patients (73%); 17and 7 patients remain any-drug free or on azathioprine only, respectively.

Conclusion: Discontinuation of successful anti-TNF treatment is frequently associated with durable very long-term remission in severe BD. Additional studies are needed since relapses not responding to anti-TNF re-treatment may occur.

退出抗肿瘤坏死因子治疗后,白塞病的长期缓解超过复发:一项结果研究的重新评估。
背景:抗肿瘤坏死因子治疗的引入大大改善了白塞病(BD)的预后。慢性炎症性关节炎或肠道疾病患者停用抗tnf治疗与亚群患者的持续缓解相关。在此,我们研究了BD患者停用TNF抑制剂后非常长时间静止的可能性。方法:回顾性纵向结果单中心研究,重点关注自2001年以来停止成功抗TNF治疗的BD患者。终点是停药后5年持续临床缓解的比例。结果:33例非生物治疗难治性重度BD患者(平均年龄47.5±11.5岁,55%为男性)实现了TNF抑制剂诱导的缓解,中位时间为2年(IQR[1-2.6])。TNF抑制剂用于视力威胁疾病(28/ 33,82%),粘膜皮肤(3/33),中枢神经系统(2/33)和胃肠道(1/33)。停药后,33例患者中有15例BD持续缓解6.6 - 20.6年(平均13.5±3.8年)。相反,18/33例患者在停药后中位9.5个月后复发[IQR 8-12,范围4-32],但13/18例患者再次使用TNF抑制剂治疗有效。其中,9/13患者第二次停药并再次达到研究终点,缓解期中位数为7.4年([IQR 5-9.3,范围5-15年)。24/33例患者(73%)达到研究终点;分别有17例和7例患者不使用任何药物或仅使用硫唑嘌呤。结论:停止成功的抗肿瘤坏死因子治疗通常与严重双相障碍患者持久的长期缓解有关。由于复发对抗肿瘤坏死因子再治疗无反应,需要进一步的研究。
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来源期刊
Rheumatology International
Rheumatology International 医学-风湿病学
CiteScore
7.30
自引率
5.00%
发文量
191
审稿时长
16. months
期刊介绍: RHEUMATOLOGY INTERNATIONAL is an independent journal reflecting world-wide progress in the research, diagnosis and treatment of the various rheumatic diseases. It is designed to serve researchers and clinicians in the field of rheumatology. RHEUMATOLOGY INTERNATIONAL will cover all modern trends in clinical research as well as in the management of rheumatic diseases. Special emphasis will be given to public health issues related to rheumatic diseases, applying rheumatology research to clinical practice, epidemiology of rheumatic diseases, diagnostic tests for rheumatic diseases, patient reported outcomes (PROs) in rheumatology and evidence on education of rheumatology. Contributions to these topics will appear in the form of original publications, short communications, editorials, and reviews. "Letters to the editor" will be welcome as an enhancement to discussion. Basic science research, including in vitro or animal studies, is discouraged to submit, as we will only review studies on humans with an epidemological or clinical perspective. Case reports without a proper review of the literatura (Case-based Reviews) will not be published. Every effort will be made to ensure speed of publication while maintaining a high standard of contents and production. Manuscripts submitted for publication must contain a statement to the effect that all human studies have been reviewed by the appropriate ethics committee and have therefore been performed in accordance with the ethical standards laid down in an appropriate version of the 1964 Declaration of Helsinki. It should also be stated clearly in the text that all persons gave their informed consent prior to their inclusion in the study. Details that might disclose the identity of the subjects under study should be omitted.
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